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Warren, ST: Mapping the vasopressin V2 receptor gene near nephrogenic diabetes insipidus. Dysmorphology and Clinical Genetics 6:203-205 (1992). |
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Riggins, GJ, Lokey, LK, Chastain, JL, Leiner, HA, Sherman, SL, Wilkinson, KD and Warren, ST: Human genes containing polymorphic trinucleotide repeats. Nature Genetics 2:186-191 (1992).Warren, ST: Advances in human molecular genetics influence clinical genetic practice. Dysmorphology and Clinical Genetics 6:34-36 (1992). |
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Warren, ST: Advances in human molecular genetics influence clinical genetic practice. Dysmorphology and Clinical Genetics 6:34-36 (1992). |
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Sutcliffe, JS, Nelson, DL, Zhang, F, Pieretti, M, Caskey, CT, Saxe, D and Warren, ST: DNA methylation represses FMR-1 transcription in fragile X syndrome. Human Molecular Genetics 1:397-400 (1992).
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Sutcliffe, JS, Zhang, F, Nelson, DL, Caskey, CT and Warren, ST: PCR amplification and analysis of yeast artificial chromosomes. Genomics 13:1303-1306 (1992).
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Van den Ouweland, Knoop, MT, Knoers, VVAM, Markslag, PWB, Rocchi, M. Warren, ST, Mandel, JL, Ropers, HH, Fahrenholz, F, Monnens, LAH and van Oost, BA: Colocalization of the gene for nephrogenic diabetes insipidus and the vasopressin type-2 receptor gene in the Xq28 region. Genomics 13:1350-1352 (1992).
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Willems, PJ, Vits, L, Raeymaekers, P, Beuten, J, Beuten, J, Coucke, P, Holden, JJA, Van Broeckhoven, CV, Warren, ST, Sagi, M, Robinson, D, Dennis, N, Friedman, J, Magnay, D, Lyonnet, S, White, BN, Wittwer, BH, Aylsworth, AS and Reicke, S: Further localization of X-linked hydrocephalus in the chromosomal region Xq28. American Journal of Human Genetics 51:307-315 (1992).
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Traupe, H, van den Ouweland, AMW, van Oost, BA, Vogel, W, Vetter, U, Warren, ST, Rocchi, M, Darlison, MG and Roppers, HH: Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel. Genomics 13:481-483 (1992).
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Riggins, GJ, Sherman, SL, Oostra, BA, Sutcliffe, JS, Feitell, D, Nelson, DL, van Oost, BA, Smits, APT, Ramos, FJ, Pfender, E, Kuhl, D, Caskey, CT and Warren, ST: Characterization of a highly polymorphic dinucleotide repeat 150 kb proximal to the fragile X site. American Journal of Medical Genetics 43:237-243 (1992).
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Verkerk, AJMH, de Vries, BBA, Niermeijer, MF, Nelson, DL, Warren, ST, Majoor-Krakauer, DF, Halley, DJJ and Oostra, BA: An intragenic probe used for diagnostics in fragile X families. American Journal of Medical Genetics 43:192-196 (1992).
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Consalez, GG, Stayton, CL, Freimer, NB, Goonewardena, Brown, WT, Gilliam, TC and Warren, ST: Isolation and characterization of a highly polymorphic human locus (DXS 455) in proximal Xq28. Genomics 12:710-714 (1992).
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